Data / Medical devices / China / Ningbo Longwell Baby Products Co Ltd
Ningbo Longwell Baby Products Co Ltd: FDA-registered device maker in Ningbo Zhejiang, China, 1 510(k) clearance
Ningbo Longwell Baby Products Co Ltd is registered with the FDA (registration 3009109684) in Ningbo Zhejiang, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 1, 2010. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009109684
- Address
- No.77 Lane 520 Tongning Road Hong Tang, Ningbo Zhejiang, China, 315033
- Owner or operator
- Ningbo Longwell Baby & Beauty Products Co Ltd (10036257)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 26, 2011
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dispenser, Liquid Medication | KYX | 1 | Manufacturer | accessdata.fda.gov |
| Nipple, Lambs Feeding | FNN | 1 | Contract manufacturer | accessdata.fda.gov |
| Pump, Breast, Non-Powered | HGY | 1 | Contract manufacturer | accessdata.fda.gov |
| Ring, Teething, Fluid-Filled | KKO | 2 | Manufacturer | accessdata.fda.gov |
| Ring, Teething, Non-Fluid Filled | MEF | 1 | Contract manufacturer | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Contract manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 1, 2010 | K092494 | GEL FILLED GUM SOOTHER | KKO | Substantially Equivalent | Luv N' Care, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Toothbrush, Manual
- All makers of Pump, Breast, Non-Powered
- All makers of Ring, Teething, Non-Fluid Filled
- All makers of Nipple, Lambs Feeding
- All makers of Dispenser, Liquid Medication
- All makers of Ring, Teething, Fluid-Filled
Updated March 1, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.